FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODEL 900S INTRAOCULAR PROBE
K Number: K812219
·
Decision Nov 16, 1981
Classifications
1
FEI Numbers
60
Registration Numbers
61
Same Product Code
179
Applicant Total
43
Review Days
102
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Basic Information
- Device Name
- MODEL 900S INTRAOCULAR PROBE
- K Number
- K812219
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4390
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Lumenis, Inc.
- Date Received
- August 6, 1981
- Decision Date
- November 16, 1981
- Product Code
- HQF
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HQF | Laser, Ophthalmic | FDA class 2 | Ophthalmic |
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